Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology

Medpace; Cincinnati (OH); On-site; USD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking a dynamic Associate Clinical Trial Manager with a PhD in Life Sciences to join their Cincinnati team. This full-time, office-based position offers recent graduates a unique opportunity to transition into the clinical research field, where they will receive comprehensive training and work alongside experienced professionals. The role involves managing clinical trial activities, ensuring quality control, and collaborating with global teams. With a commitment to innovation and patient care, this company provides a supportive environment for career growth and development in the exciting field of therapeutics.

Benefits

Competitive Benefits

Flexible Work Options

Community Involvement Initiatives

Qualifications

• PhD graduates with a focus on Nephrology and clinical trial management.
• Ability to thrive in a fast-paced, international environment.

Responsibilities

• Collaborate on global study activities with project teams.
• Ensure timely completion of tasks and maintain project status reports.
• Oversee quality control of regulatory filings and manage study logistics.

Skills

Analytical Skills

Project Management

Communication

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology

Job Locations: United States - OH - Cincinnati | United States - TX - Irving (Dallas) | United States - CO - Denver

Job Summary

Medpace is seeking candidates with Nephrology-related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM). The aCTM will work with the Clinical Trial Management team alongside Project Coordinators and Clinical Trial Managers to perform clinical trial management activities. Candidates should have a desire to apply their analytical and academic skills in clinical project administration and management.

This role offers a great opportunity for recent PhD graduates to enter the industry, receive comprehensive training, work internationally, and develop a career in the research and development of innovative therapeutics. Expect an intensive training period and demonstrate the motivation for rapid career progression into Clinical Trial Management (CTM).

Responsibilities

• Communicate and collaborate on global study activities with project teams
• Ensure timely and accurate completion of recurrent tasks
• Maintain project-specific status reports in the clinical trial management system
• Interact with internal teams, sponsors, study sites, and vendors
• Oversee and ensure quality control of regulatory filings
• Manage study supplies and logistics
• Create and update project timelines
• Coordinate meetings and document minutes

Qualifications

• PhD in Life Sciences
• Ability to work in a fast-paced, international environment
• Experience in CRO or pharmaceutical industry is a plus but not required

Medpace Overview

Medpace is a full-service clinical CRO providing Phase I-IV development services globally. Our mission is to accelerate the development of safe and effective therapeutics through scientific rigor and discipline, leveraging expertise across various therapeutic areas. Headquartered in Cincinnati, Ohio, with over 5,000 employees worldwide.

Why Join Medpace?

Join us to make a difference in patients' lives. We offer a dynamic work environment, competitive benefits, and opportunities for professional growth. Our Cincinnati campus features modern amenities, flexible work options, and community involvement initiatives.

Awards & Recognition

• Top Workplace 2024 - Cincinnati Enquirer
• Forbes America's Most Successful Midsize Companies 2021-2024
• CRO Leadership Awards from Life Science Leader magazine

Next Steps

Qualified candidates will be reviewed, and if interested, contacted for further steps.

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